Thank you for everything! before long i will start my journey, and keep playing the lottery in the hope i can afford a better doctor ,mine is useless ,doesnt know much about hep c ,saying that there is alot of doctors out there that do know about this, and free, as for the health service you get whats paid for i suppose , stay well john
Just a quick note to say hi! nice to hear the chills have gone, in this country england,we call it the N H S (national health service)its free, there is of course BUPA but its not cheap, its more of a private sector, for those that can afford the lavish lifestyles ,like footballers ,singers, actors,im sure theres one similar in your neck of the woods
Just a quick note to say hi! thank you,im gonna keep bugging my doc until he gives in and sorts my tx out,or at least brings it a little closer,ive got no insurance either,difficult to get with this dragon,(wrong really),time to break out the awareness flags and shame them into submission,anyway ,its time to get on the phone,and bug my doc, speak soon, john
Like you, I am also just about to start treatment - in my case it's Tuesday next week. And yes, the reported side effects sound scary. But, the alternative is NO treatment, and where will that get us? So - believe in the treatment and in your ability to handle it. I'm trying to do just that too, All the best, Inge
Thank you for everything! thank you for replying,its only been one month,so ive still got time yet
FYI: HCV Advocate Site says that there is a support group in Hawaii.
Hope you are well!